Joo Myun PARK1* and Sung Hoi HUH2

Total Page:16

File Type:pdf, Size:1020Kb

Joo Myun PARK1* and Sung Hoi HUH2 ACTA ICHTHYOLOGICA ET PISCATORIA (2015) 45 (4): 427–431 DOI: 10.3750/AIP2015.45.4.13 LENGTH–WEIGHT RELATIONS FOR 29 DEMERSAL FISHES CAUGHT BY SMALL OTTER TRAWL ON THE SOUTH-EASTERN COAST OF KOREA Joo Myun PARK1* and Sung Hoi HUH2 1Department of Biological Sciences, Macquarie University, Sydney, Australia 2Department of Oceanography, Pukyong National University, Busan, Korea Park J.M., Huh S.H. 2015. Length–weight relations for 29 demersal fi shes caught by small otter trawl on the south-eastern coast of Korea. Acta Ichthyol. Piscat. 45 (4): 427–431. Abstract. We present herewith the relations between total length and weight (LWRs) for 29 fi sh species from the southern coast of the East Sea (=Sea of Japan), Korea: Conger myriaster (Brevoort, 1856); Coilia nasus Temminck et Schlegel, 1846; Engraulis japonicus Temminck et Schlegel, 1846; Clupea pallasii pallasii Valenciennes, 1847; Coelorinchus multispinulosus Katayama, 1942; Lophius litulon (Jordan, 1902); Zeus faber Linnaeus, 1758; Paracentropogon rubripinnis (Temminck et Schlegel, 1843); Lepidotrigla guentheri Hilgendorf, 1879; Liparis tanakae (Gilbert et Burke, 1912); Acropoma japonicum Günther, 1859; Doederleinia berycoides (Hilgendorf, 1879); Jaydia lineata (Temminck et Schlegel, 1842); Ostorhinchus semilineatus (Temminck et Schlegel, 1842); Sillago sihama (Forsskål, 1775); Trachurus japonicus (Temminck et Schlegel, 1844); Pagrus major (Temminck et Schlegel, 1843); Pennahia argentata (Houttuyn, 1782); Zoarces gillii Jordan et Starks, 1905; Callionymus lunatus Temminck et Schlegel, 1845; Callionymus valenciennei Temminck et Schlegel, 1845; Am- blychaeturichthys hexanema (Bleeker, 1853); Amblychaeturichthys sciistius (Jordan et Snyder, 1901); Sphyraena pinguis Günther, 1874; Trichiurus lepturus Linnaeus, 1758; Psenopsis anomala (Temminck et Schlegel, 1844); Pseudorhombus pentophthalmus Günther, 1862; Pseudopleuronectes yokohamae (Günther, 1877); and Cyno- glossus robustus Günther, 1873. The LWRs for 12 species are estimated for the fi rst time and new maximum lengths for six species are reported herewith. All of the relations between total length and weight were signifi cant (all r2 > 0.938). The values of exponent b, estimated using simple linear least squares of log-transformed weight and length data, ranged from 2.730 to 3.440. Keywords: marine fi sh, fi sheries management, East Sea, Sea of Japan, LWR The fi shes examined in the presently reported study habitats and/or regions (Gonçalves et al. 1997). Although were collected off the south-eastern coast of Korea. The LWRs of scorpionfi shes and righteye fl ounders inhabiting study area, in terms of its environmental and geographical south-eastern coast of Korea have been reported (Baeck characteristics, differs generally from other coastal marine et al. 2012, 2014), there are still insuffi cient informa- ecosystems in the east and south seas of Korea (Suh et tion of LWR parameters for Korean fi shes. This study al. 2001). It is a habitat for many commercially important reports LWRs for 29 fi sh species collected by demersal demersal fi sh species and has been renowned for being trawl from the south-eastern coast of Korea: Conger abundant in prey organisms (Kim unpublished**). How- myriaster (Brevoort, 1856); Coilia nasus Temminck et ever, little is known on the ecology of the fi shes living in Schlegel, 1846; Engraulis japonicus Temminck et Schle- the area. gel, 1846; Clupea pallasii pallasii Valenciennes, 1847; Length–weight relation (LWR) parameters (a, b) are Coelorinchus multispinulosus Katayama, 1942; Lophius useful in the assessment of fi sh stocks and populations litulon (Jordan, 1902); Zeus faber Linnaeus, 1758; (Ricker 1968, Froese 2006). LWRs are used to estimate the Paracentropogon rubripinnis (Temminck et Schlegel, mean weight for a given length group and convert length 1843); Lepidotrigla guentheri Hilgendorf, 1879; Liparis observations into weights to provide a measure of biomass tanakae (Gilbert et Burke, 1912); Acropoma japonicum (Froese 2006, Froese et al. 2011). LWRs also allow for life Günther, 1859; Doederleinia berycoides (Hilgendorf, history and morphological comparisons between different 1879); Jaydia lineata (Temminck et Schlegel, 1842); Os- fi sh species or between fi sh populations from different torhinchus semilineatus (Temminck et Schlegel, 1842); * Correspondence: Dr Joo Myun Park, Department of Biological Sciences, Macquarie University, Sydney, NSW 2109, Australia; phone: +61 2 9850 8234; e-mail: (JMP) [email protected] or [email protected], (SHH) [email protected] ** Kim D.J. 1998. [Seasonal variation of species composition of demersal fi sh off Kori.] MSc Thesis, Pukyong National University, Korea. [In Korean.] 428 Park and Huh Sillago sihama (Forsskål, 1775); Trachurus japonicus hama. All of b values were within the expected range of (Temminck et Schlegel, 1844); Pagrus major (Temminck 2.5 to 3.5 (Froese 2006). The mean value of b (± stan- et Schlegel, 1843); Pennahia argentata (Houttuyn, 1782); dard deviation) was 3.117 ± 0.184 indicating a tenden- Zoarces gillii Jordan et Starks, 1905; Callionymus lunatus cy towards positive allometry, which is followed by the Temminck et Schlegel, 1845; Callionymus valenciennei majority of fi sh species (Froese 2006). The LWRs for 12 Temminck et Schlegel, 1845; Amblychaeturichthys of the 29 species determined in the course of the pres- hexanema (Bleeker, 1853); Amblychaeturichthys sciisti- ently reported study are fi rst reports of LWRs for those us (Jordan et Snyder, 1901); Sphyraena pinguis Günther, species. For remaining 17 species, LWRs of 8 species, 1874; Trichiurus lepturus Linnaeus, 1758; Psenopsis Amblychaeturichthys hexanema, Jaydia lineata, Conger anomala (Temminck et Schlegel, 1844); Pseudorhombus myriaster, Engraulis japonicus, Liparis tanakae, Lophi- pentophthalmus Günther, 1862; Pseudopleuronectes us litulon, Pseudopleuronectes yokohamae, and S. siha- yokohamae (Günther, 1877); and Cynoglossus robustus ma have been reported from the Yellow Sea (Xue et al. Günther, 1873. 2011, Wang et al. 2013) and the southern coast of Korea Fish specimens were collected monthly from January (Baeck et al. 2014). The LWRs of 15 species also were to December 2006 off the south-eastern coast of Korea available in FishBase (Froese and Pauly 2015), and 2 (35°15′~35°17′N, 129°18′~129°21′E) from depths be- species, A. hexanema and L. litulon were only listed in tween 30 and 60 m using a small otter trawl. Fish samples the literature (Xue et al. 2011, Wang et al. 2013). were immediately packed with ice and taken to the labora- The seasonal LWRs for 10 of the 29 species are present- tory for measurement of total length (TL) and wet weight ed in Table 2. The parameter b did not differ signifi cant- to the nearest millimetre and gram, respectively. All scien- ly (ANCOVA; P > 0.05) with seasons for Jaydia lineata, tifi c names were verifi ed following FishBase (Froese and Coelorinchus multispinulosus, Lophius litulon, Trachurus Pauly 2015). japonicus, Callionymus lunatus, and Pseudopleuronectes For each species, the weight–length relation was deter- yokohamae, whereas it differed signifi cantly (ANCOVA; mined based on the formula: P < 0.05) for Acropoma japonicum, Clupea pallasii palla- sii, Liparis tanakae, and Pseudorhombus pentophthalmus. W = aLb Lower b values were recorded in winter for C. pallasii pallasii, while A. japonicum in summer and winter, and where W is the wet weight [g], L is total length [cm], P. pentophthalmus were in summer. For L. tanakae, the b and a and b are the intercept and allometric coeffi cient, value was lower in autumn than other seasons. Seasonal respectively. Parameters a and b were estimated using differences in length–weight relations may be due to sea- a simple linear regression analysis of log-transformed sonal difference in the condition and/or sexual maturing data. Extreme outliers were removed before fi tting the of the specimens (Moutopoulos and Stergiou 2002, Froese linear regression (Froese et al. 2011). The 95% confi - 2006). dence intervals (CIs) of parameters a and b and the sta- Our LWR estimates were compared with the Bayesian tistical signifi cance level of r2 were estimated using SYS- estimates of LWRs in fi shes (Froese et al. 2014) and were TAT software (Systat, version 12. SPSS, USA). LWRs found to fall within the ranges expected for each species were summarized over all months. Seasonal LWRs, each or the genus and body shape where they belong. Thus, our spring (March–May), summer (June–August), autumn results represent the reasonable estimates of the LWRs for (September–November), and winter (December–Febru- the 29 species. The estimated parameters of LWRs in this ary), were also estimated for species where more than work should be used with some caution as the length rang- 30 specimens were collected for each season. Analysis es of the specimens available was limited by the selective of covariance (ANCOVA) was used to determine signif- characteristics of fi shing gear used. The majority of the icant differences in the slopes of length–weight regres- samples did not include the full size ranges of specimens sions between seasons. in the study area, especially early juveniles. Petrakis and Length–weight regressions were applied to 16 456 Stergiou (1995) suggested the use of LWRs only for spec- specimens of the 29 species from 24 families. Comparing imens of lengths within the length ranges used in the esti- with information in FishBase (Froese and Pauly 2015), our mation of the parameters. results provide new maximum lengths for 6 species:
Recommended publications
  • Art. Marcinkevicius
    Revista de Biología Marina y Oceanografía Vol. 48, Nº2: 285-292, agosto 2013 DOI 10.4067/S0718-19572013000200008 Article Early life history of three Patagonian zoarcids Desarrollo de los estadios tempranos de tres zoarcidos Patagónicos Mauro S. Marcinkevicius1 and Atila E. Gosztonyi2 1Instituto de Desarrollo Costero, Universidad Nacional de la Patagonia San Juan Bosco, Ciudad Universitaria, Comodoro Rivadavia, Km 4, Chubut, Argentina, CP (9005). [email protected] 2Centro Nacional Patagónico, CONICET, Puerto Madryn Bvd. Brown 2915, U9120ACD, Puerto Madryn, Chubut, Argentina Resumen.- Los zoárcidos están bien representados en la zona intermareal de la costa Patagónica. Se conoce que son ovíparos con cuidado parental, pero hay poca información del desarrollo ontogenético. El objetivo de este trabajo fue describir los estadios de desarrollo temprano de 3 especies de zoárcidos patagónicos: Iluocoetes elongatus, Phucocoetes latitans y Dadyanos insignis. Se muestrearon masas de huevos de estas 3 especies, en la zona intermareal de la Ría Deseado (Santa Cruz, Argentina). Los huevos fueron depositados en acuarios y condiciones controladas para obtener las postlarvas y los estadios siguientes. Los huevos más grandes obtenidos fueron de I. elongatus con 4,94 mm de diámetro, 4,93 mm en D. insignis y 4,20 mm en P. latitans. Las postlarvas eclosionaron con un alto grado de desarrollo (tamaño de eclosión 17,5 mm de longitud estándar (LS) en I. elongatus, 18 mm LS en P. latitans y 22 mm LS en D. insignis), difiriendo de los juveniles por la presencia del saco vitelino. El patrón de pigmentación corresponde al de los adultos y durante el desarrollo se intensifica.
    [Show full text]
  • Evolutionary Affinities of the Unfathomable Parabrotulidae
    Molecular Phylogenetics and Evolution 109 (2017) 337–342 Contents lists available at ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev Short Communication Evolutionary affinities of the unfathomable Parabrotulidae: Molecular data indicate placement of Parabrotula within the family Bythitidae, Ophidiiformes ⇑ Matthew A. Campbell a,b, , Jørgen G. Nielsen c, Tetsuya Sado d, Chuya Shinzato e, Miyuki Kanda f, ⇑ Takashi P. Satoh g, Masaki Miya d, a Department of Ecology and Evolutionary Biology, University of California Santa Cruz, Santa Cruz, CA 95064, USA b Fisheries Ecology Division, Southwest Fisheries Science Center, National Marine Fisheries Service, Santa Cruz, CA 95060, USA c Natural History Museum of Denmark, University of Copenhagen, Universitetsparken 15, DK-2100 Copenhagen Ø, Denmark d Department of Ecology and Environmental Sciences, Natural History Museum and Institute, Chiba 260-8682, Japan e Marine Genomics Unit, Okinawa Institute of Science and Technology Graduate University, Okinawa 904-0485, Japan f DNA Sequencing Section, Okinawa Institute of Science and Technology Graduate University, Okinawa 904-0485, Japan g Seto Marine Biological Laboratory, Field Science Education and Research Center, Kyoto University, 459 Shirahama, Nishimuro, Wakayama 649-2211, Japan article info abstract Article history: Fishes are widely diverse in shape and body size and can quite rapidly undergo these changes. Received 3 November 2016 Consequently, some relationships are not clearly resolved with morphological analyses. In the case of Revised 30 January 2017 fishes of small body size, informative characteristics can be absent due to simplification of body struc- Accepted 2 February 2017 tures. The Parabrotulidae, a small family of diminutive body size consisting of two genera and three spe- Available online 6 February 2017 cies has most recently been classified as either a perciform within the suborder Zoarcoidei or an ophidiiform.
    [Show full text]
  • Delaware's Wildlife Species of Greatest Conservation Need
    CHAPTER 1 DELAWARE’S WILDLIFE SPECIES OF GREATEST CONSERVATION NEED CHAPTER 1: Delaware’s Wildlife Species of Greatest Conservation Need Contents Introduction ................................................................................................................................................... 7 Regional Context ........................................................................................................................................... 7 Delaware’s Animal Biodiversity .................................................................................................................... 10 State of Knowledge of Delaware’s Species ................................................................................................... 10 Delaware’s Wildlife and SGCN - presented by Taxonomic Group .................................................................. 11 Delaware’s 2015 SGCN Status Rank Tier Definitions................................................................................. 12 TIER 1 .................................................................................................................................................... 13 TIER 2 .................................................................................................................................................... 13 TIER 3 .................................................................................................................................................... 13 Mammals ....................................................................................................................................................
    [Show full text]
  • COMMON NAME SCIENTIFIC NAME BYCATCH UNIT CV FOOTNOTE(S) Mid-Atlantic Bottom Longline American Lobster Homarus Americanus 35.43 P
    TABLE 3.4.2a GREATER ATLANTIC REGION FISH BYCATCH BY FISHERY (2015) Fishery bycatch ratio = bycatch / (bycatch + landings). These fisheries include numerous species with bycatch estimates of 0.00; these 0.00 species are listed in Annexes 1-3 for Table 3.4.2a. All estimates are live weights. 1, 4 COMMON NAME SCIENTIFIC NAME BYCATCH UNIT CV FOOTNOTE(S) Mid-Atlantic Bottom Longline American lobster Homarus americanus 35.43 POUND 1.41 t Gadiformes, other Gadiformes 2,003.72 POUND .51 o, t Jonah crab Cancer borealis 223.42 POUND .67 t Monkfish Lophius americanus 309.83 POUND .49 e, f Night shark Carcharhinus signatus 593.28 POUND .7 t Offshore hake Merluccius albidus 273.33 POUND 1.41 Ray-finned fishes, other (demersal) Actinopterygii 764.63 POUND .64 o, t Red hake Urophycis chuss 313.85 POUND 1.39 k Scorpionfishes, other Scorpaeniformes 10.12 POUND 1.41 o, t Shark, unc Chondrichthyes 508.53 POUND .7 o, t Skate Complex Rajidae 27,670.53 POUND .34 n, o Smooth dogfish Mustelus canis 63,484.98 POUND .68 t Spiny dogfish Squalus acanthias 32,369.85 POUND 1.12 Tilefish Lopholatilus chamaeleonticeps 65.80 POUND 1.41 White hake Urophycis tenuis 51.63 POUND .85 TOTAL FISHERY BYCATCH 129,654.74 POUND TOTAL FISHERY LANDINGS 954,635.64 POUND TOTAL CATCH (Bycatch + Landings) 1,084,290.38 POUND FISHERY BYCATCH RATIO (Bycatch/Total Catch) 0.12 Mid-Atlantic Clam/Quahog Dredge American lobster Homarus americanus 4,853.05 POUND .95 t Atlantic angel shark Squatina dumeril 5,313.55 POUND .96 t Atlantic surfclam Spisula solidissima 184,454.52 POUND .93 Benthic
    [Show full text]
  • Marine Biodiversity: Responding to the Challenges Posed by Climate Change, Fisheries, and Aquaculture
    e Royal Society of Canada Expert Panel Sustaining Canada’s Marine Biodiversity: Responding to the Challenges Posed by Climate Change, Fisheries, and Aquaculture REPORT February 2012 Prof. Isabelle M. Côté Prof. Julian J. Dodson Prof. Ian A. Fleming Prof. Je rey A. Hutchings (Chair) Prof. Simon Jennings Prof. Nathan J. Mantua Prof. Randall M. Peterman Dr. Brian E. Riddell Prof. Andrew J. Weaver, FRSC Prof. David L. VanderZwaag SUSTAINING CANADIAN MARINE BIODIVERSITY An Expert Panel Report on Sustaining Canada's Marine Biodiversity: Responding to the Challenges Posed by Climate Change, Fisheries, and Aquaculture Prepared by: The Royal Society of Canada: The Academies of Arts, Humanities and Sciences of Canada February 2012 282 Somerset Street West, Ottawa ON, K2P 0J6 • Tel: 613-991-6990 • www.rsc-src.ca | 1 Members of the Expert Panel on Sustaining Canadian Marine Biodiversity Isabelle M. Côté, Professor, Department of Biological Sciences, Simon Fraser University Julian J. Dodson, Professeur titulaire, Département de biologie, Université Laval Ian A. Fleming, Professor, Ocean Sciences Centre, Memorial University of Newfoundland Jeffrey A. Hutchings, Killam Professor and Canada Research Chair in Marine Conservation and Biodiversity, Department of Biology, Dalhousie University Panel Chair Simon Jennings, Principal Scientist, Centre for Environment, Fisheries and Aquaculture Science (CEFAS), Lowestoft, UK, and Honorary Professor of Environmental Sciences at the University of East Anglia, UK Nathan J. Mantua, Associate Research Professor, Aquatic and Fisheries Sciences, University of Washington, USA Randall M. Peterman, Professor and Canada Research Chair in Fisheries Risk Assessment and Management, School of Resource and Environmental Management, Simon Fraser University Brian E. Riddell, PhD, CEO, Pacific Salmon Foundation, Vancouver, British Columbia Andrew J.
    [Show full text]
  • Embryonic Growth During Gestation of the Viviparous Eelpout, Zoarces Elongatus Yasunori Koya,1 Toshitaka Ikeuchi,2 Takahiro Mats
    Japan. J. Ichthyol. 魚 類 学 雑 誌 41 (3): 338-342, 19 94 41 (3): 338-342, 1 9 94 mation pertaining to this subject was available. Embryonic Growth during Gestation of the n the present study, the changes inI total length, Viviparous Eelpout, Zoarces elongatus body weight and dry weight were investigated as criteria for growth during gestation in Z. elongatus. Yasunori Koya,1 Toshitaka Ikeuchi,2 In addition, tracer experiments on the mechanism Takahiro Matsubara,1 Shinji Adachi2 and site of nutrient absorption by the embryo were and Kohei Yamauchi2 performed. Hokkaido National Fisheries1 Research Institute, 116 Katsurakoi, Kushiro, Hokkaido 085, Japan Materials and Methods 2Department of Biology, Faculty of Fisheries, Female Zoarces elongatus were caught by angling Hokkaido University,3-1-1 Minato-cho, in Akkeshi Bay, eastern Hokkaido, Japan, during Hakodate, Hokkaido041, Japan May to October 1992. Thirty-four fish were subse- (ReceivedJuly 20, 1994;in revisedform September13, 1994; quently transferred to Usujiri Fisheries Laboratories, acceptedOctober 14, 1994) Hokkaido University, and kept in an indoor 1000 liter circular tank with flowing sea water under nat- ural photoperiod conditions. At monthly intervals The viviparous mode of reproduction in teleosts during the gestation period (September to February, was categorized as lecithotrophy and matrotrophy Koya et al., 1993), four to ten females were anesthe- on the basis of maternal-fetal trophic relationships tized with ethyl 4-aminobenzoate and the ovaries (Wourms, 1981). Lecithotrophic embryos derive removed. Embryos were removed from the ovaries their nutrition solely from yolk reserves, whereas and the total lengths and wet weights measured, matrotrophic embryos depend on a supply of mater- before being dried for 48 hr at 80•Ž.
    [Show full text]
  • The Ocean Genome: Conservation and the Fair, Equitable and Sustainable Use of Marine Genetic Resources
    Commissioned by BLUE PAPER The Ocean Genome: Conservation and the Fair, Equitable and Sustainable Use of Marine Genetic Resources LEAD AUTHORS Robert Blasiak, Rachel Wynberg, Kirsten Grorud-Colvert and Siva Thambisetty CONTRIBUTING AUTHORS Narcisa M. Bandarra, Adelino V.M. Canário, Jessica da Silva, Carlos M. Duarte, Marcel Jaspars, Alex D. Rogers, Kerry Sink and Colette C.C. Wabnitz oceanpanel.org About the High Level Panel for a Sustainable Ocean Economy The High Level Panel for a Sustainable Ocean Economy (Ocean Panel) is a unique initiative by 14 world leaders who are building momentum for a sustainable ocean economy in which effective protection, sustainable production and equitable prosperity go hand in hand. By enhancing humanity’s relationship with the ocean, bridging ocean health and wealth, working with diverse stakeholders and harnessing the latest knowledge, the Ocean Panel aims to facilitate a better, more resilient future for people and the planet. Established in September 2018, the Ocean Panel has been working with government, business, financial institutions, the science community and civil society to catalyse and scale bold, pragmatic solutions across policy, governance, technology and finance to ultimately develop an action agenda for transitioning to a sustainable ocean economy. Co-chaired by Norway and Palau, the Ocean Panel is the only ocean policy body made up of serving world leaders with the authority needed to trigger, amplify and accelerate action worldwide for ocean priorities. The Ocean Panel comprises members from Australia, Canada, Chile, Fiji, Ghana, Indonesia, Jamaica, Japan, Kenya, Mexico, Namibia, Norway, Palau and Portugal and is supported by the UN Secretary-General's Special Envoy for the Ocean.
    [Show full text]
  • Ålekvabbe, Zoarces Viviparus
    Atlas over danske saltvandsfisk Ålekvabbe Zoarces viviparus (Linnaeus, 1758) Af Henrik Carl & Peter Rask Møller Ålekvabbe fra mundingen af Ribe Vesterå, 29. oktober 2009. © Henrik Carl. Projektet er finansieret af Aage V. Jensen Naturfond Alle rettigheder forbeholdes. Det er tilladt at gengive korte stykker af teksten med tydelig kildehenvisning. Teksten bedes citeret således: Carl, H. & Møller, P.R. 2019. Ålekvabbe. I: Carl, H. & Møller, P.R. (red.). Atlas over danske saltvandsfisk. Statens Naturhistoriske Museum. Online- udgivelse, december 2019. Systematik og navngivning Arten blev oprindelig beskrevet under navnet Blennius viviparus – altså som tilhørende slimfiskefamilien Blenniidae. Senere blev den flyttet til ålekvabbefamilien Zoarcidae Swainson, 1839 og slægten Zoarces Cuvier, 1829. Zoarces er den eneste slægt i underfamilien Zoarcinae (Eschmeyer & Fong 2019) og den omfatter nu seks arter, med fire i den nordlige del af Stillehavet og to i den nordlige del af Atlanterhavet (Anderson & Fedorov 2004; Parin et al. 2005; Chereshney et al. 2007; Froese & Pauly 2019). I Atlanterhavet drejer det sig foruden den almindelige ålekvabbe også om den vestatlantiske ålekvabbe (Zoarces americanus), der med en maksimalstørrelse på 110 cm og 5,4 kg er slægtens største art (Leim & Scott 1966; Robins & Ray 1986). Genetiske og morfologiske undersøgelser placerer den almindelige ålekvabbe i en gruppe sammen med aflang ålekvabbe (Z. elongatus), Fedorovs ålekvabbe (Z. fedorovi) og Andriashevs ålekvabbe (Z. andriashevi), mens vestatlantisk ålekvabbe og japansk ålekvabbe (Z. gillii) udgør en anden gruppe (Radchenko et al. 2010). Det officielle danske navn er almindelig ålekvabbe, men i de fleste sammenhænge kaldes den blot for ålekvabbe (Carl et al. 2004). Krøyer (1838-40) brugte navnet den levendefødende ålekvabbe, og han nævner, at den herhjemme var forsynet med en hel del navne som ålekvabbe, ålekone, ålemoder, ålekuse, åltøjte, åleknude osv.
    [Show full text]
  • Laboratory Observations of Reproduction in the Deep-Water Zoarcids Lycodes Cortezianus and Lycodapus Mandibularis (Teleostei: Zoarcidae)1
    Laboratory Observations of Reproduction in the Deep-Water Zoarcids Lycodes cortezianus and Lycodapus mandibularis (Teleostei: Zoarcidae)1 Lara A. Ferry-Graham,2,3 Jeffrey C. Drazen,4 and Veronica Franklin5 Abstract: The first observations of reproduction and associated behaviors in captive bigfin eelpout, Lycodes cortezianus, and pallid eelpout, Lycodapus mandibu- laris, are reported here. One Lycodes cortezianus pair produced 13 transparent and negatively buoyant eggs that were approximately 6 mm in diameter. These were laid on a hydroid-covered rock. The development period was about 7 months, and the young that emerged were approximately 2 cm in total length. An addi- tional captive pair also exhibited mating behavior as the male repeatedly nudged the female and the pair produced a burrow under a sponge; however the male died before any mating. Two gravid female Lycodapus mandibularis were captured and laid between 23 and 46 eggs that were about 4 mm in diameter. These were released on the sandy substrate after the females moved the sand about the tank, and the eggs were negatively buoyant. These eggs were all unfertilized. Addi- tional burrowing behavior was observed from other captive individuals, but no eggs were subsequently produced. Taken together, our observations suggest that burrowing or use of other protective structures is a reproductive behavior of central importance to zoarcids. Contrary to some earlier hypotheses, even midwater species likely return to the sediment to burrow and/or deposit eggs. This behavior means that field data regarding reproduction in this family will continue to be difficult to obtain, and the contribution of further study in labo- ratory situations should not be underestimated.
    [Show full text]
  • Mapping Biodiversity on the Scotian Shelf and in the Bay of Fundy
    Canadian Science Advisory Secretariat (CSAS) Research Document 2016/006 Maritimes Region Mapping Biodiversity on the Scotian Shelf and in the Bay of Fundy C.A. Ward-Paige and A. Bundy Science Branch, Maritimes Region Ocean and Ecosystem Science Division Fisheries and Oceans Canada PO Box 1006, 1 Challenger Drive Dartmouth, Nova Scotia B2Y 4A2 March 2016 Foreword This series documents the scientific basis for the evaluation of aquatic resources and ecosystems in Canada. As such, it addresses the issues of the day in the time frames required and the documents it contains are not intended as definitive statements on the subjects addressed but rather as progress reports on ongoing investigations. Research documents are produced in the official language in which they are provided to the Secretariat. Published by: Fisheries and Oceans Canada Canadian Science Advisory Secretariat 200 Kent Street Ottawa ON K1A 0E6 http://www.dfo-mpo.gc.ca/csas-sccs/ [email protected] © Her Majesty the Queen in Right of Canada, 2016 ISSN 1919-5044 Correct citation for this publication: Ward-Paige, C.A., and Bundy, A. 2016. Mapping Biodiversity on the Scotian Shelf and in the Bay of Fundy. DFO Can. Sci. Advis. Sec. Res. Doc. 2016/006. v + 90 p. TABLE OF CONTENTS ABSTRACT ................................................................................................................................ iv RÉSUMÉ .................................................................................................................................... v INTRODUCTION ........................................................................................................................1
    [Show full text]
  • SPECIES INFORMATION SHEET Zoarces Viviparus
    SPECIES INFORMATION SHEET Zoarces viviparus English name: Scientific name: Eelpout / Viviparous blenny Zoarces viviparus Taxonomical group: Species authority: Class: Actinopterygii Linnaeus, 1758 Order: Perciformes Family: Zoarcidae Subspecies, Variations, Synonyms: – Generation length: 6.7 years Past and current threats (Habitats Directive Future threats (Habitats Directive article 17 article 17 codes): Climate change (M01.01), codes): Climate change (M01.01), Contaminant Contaminant pollution (H03), Competition and pollution (H03), Competition and predation (I02), predation (I02), By-catch (F02) By-catch (F02), Alien species (I01). IUCN Criteria: HELCOM Red List NT A2b Category: Near Threatened Global / European IUCN Red List Category Habitats Directive: NE/NE – Previous HELCOM Red List Category (2007): LC Protection and Red List status in HELCOM countries: Denmark –/–, Estonia –/LC, Finland –/LC, Germany –/V (Near threatened, Baltic Sea), Latvia –/–, Lithuania –/–, Poland –/–, Russia –/–, Sweden –/NT Distribution and status in the Baltic Sea region Eelpout is widely distributed and reproducing in coastal areas in the whole HELCOM area. As eelpout is not one of the most important commercial fish species, the data on its population development does not cover the whole Baltic Sea. However, in two of the four Swedish surveys available significant declines of more than 50% have been observed during the last 20 years. Despite the species being commonly used for environmental monitoring, index of abundance data is not collected in other regions. Eelpout is commercially fished in Latvia and in the Russian part of the Gulf of Finland fishermen often catch it from ice when hook-fishing smelt in spring time. There are no signals about stock decline in these areas.
    [Show full text]
  • (Lisa) Using Next Generation Sequencing Angela Bertel‑Sevilla 1, Juan F
    www.nature.com/scientificreports OPEN De novo assembly and characterization of the liver transcriptome of Mugil incilis (lisa) using next generation sequencing Angela Bertel‑Sevilla 1, Juan F. Alzate 2 & Jesus Olivero‑Verbel 1* Mugil incilis (lisa) is an important commercial fsh species in many countries, living along the coasts of the western Atlantic Ocean. It has been used as a model organism for environmental monitoring and ecotoxicological investigations. Nevertheless, available genomic and transcriptomic information for this organism is extremely defcient. The aim of this study was to characterize M. incilis hepatic transcriptome using Illumina paired-end sequencing. A total of 32,082,124 RNA-Seq read pairs were generated utilizing the HiSeq platform and subsequently cleaned and assembled into 93,912 contigs (N50 = 2,019 bp). The analysis of species distribution revealed that M. incilis contigs had the highest number of hits to Stegastes partitus (13.4%). Using a sequence similarity search against the public databases GO and KEGG, a total of 7,301 and 16,967 contigs were annotated, respectively. KEGG database showed genes related to environmental information, metabolism and organismal system pathways were highly annotated. Complete or partial coding DNA sequences for several candidate genes associated with stress responses/detoxifcation of xenobiotics, as well as housekeeping genes, were employed to design primers that were successfully tested and validated by RT-qPCR. This study presents the frst transcriptome resources for Mugil incilis and provides basic information for the development of genomic tools, such as the identifcation of RNA markers, useful to analyze environmental impacts on this fsh Caribbean species.
    [Show full text]